Only need help with #5, please. 5) Draw the product(s) of the reaction of (R)-3-chloro-1-butene with...
2. (4 pts) Draw the structures of the two possible products- 3-chloro-1-butene and 1-chloro-2- butene. What type of isomers are these two compounds?
The reaction of 3-chloro-1-butene with ethoxide ion in ethanol yields only 3-ethoxy-1-butene; the rate of this reaction depends on the concentration of both 3-chloro-1-butene and ethoxide ion. The reaction of 3-chloro-1- butene with ethanol alone, on the other hand, yields both 3-ethoxy-1-butene and 1-ethoxy-2-butene. How do you account for these different results? (0.3 pts) CH3CH2OH 3-chloro-1-butene 1-ethoxy-2-butene 3-ethoxy-1-butene CH3CH20 CH2CH2OH 3-ethoxy-1-butene
Alkyl Halides: Elimination reaction with (2R,3R)-2-chloro-3-methylpentane Draw the product formed when (2R,3R)-2-chloro-3-methylpentane under-goes an elimination reaction with NaOCH3. Alkyl Halides: Elimination reaction with 3-chloro-3-ethyl-2,2-dimethylpentane. Draw the structure of the product that is formed when 3-chloro-3-ethyl-2,2-dimethylpentane undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product. Identify the three products formed when 2-bromo-2-methylpropane is dissolved in a mixture of 80% ethanol and 20% water.
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using the scheme, determine what is your intermediate. It depends on reactants 2) Type 1: Markovnikoy, no preference for sin and anti- draw two products with wedges and dashes; check rearrangement BH TO Type 2- anti addition only, no need in HOR Markovnikov rule, no rearrangement Type 3-sin addition only, anti-Markovnikow no rearrangement CC formation-Zaltsev rule 3) After you draw products: check if product can...
Need help with the questions Circle the compound with the highest heat of combustion 2,3-dimethyl-2-butene 2-methyl-2-pentene (E) 2-hexene (Z) 2-hexene (Z) 3-methyl-2-pentene 8. What are the three hydration reactions for alkenes? What is the regiochemistry for each one? Which one(s) do(es) not go through a carbocation intermediate? 9. 10. Which compound below is more reactive towards E2 elimination? Neomenthyl Chloride Menthyl Chloride Cyclohexane 11. Draw the following structures Acetylene Acetylide lon Part 2. Roactions (Each structure is worth 5 points)....
5. Explain how the following changes will influence the rate of the reaction of 2-bromo-2- methylbutane with methanol: a. The alkyl halide is changed to 2-chloro-2-methylbutane b. The alkyl halide is changed to 2-chloro-3-methylbutane 6. What product(s) do you predict for the following reactions? Be specific with regard to stereochemistry. Also, indicate which stereoisomer will be more predominant. a. R-2-bromopentane + CH30 b. R-3-bromo-3-metylheptane + CH3OH C. 1-bromo-2-butene + CH30 d. 1-bromo-2-butene + CH3OH e. E2 reaction of 2-bromobutane f....
Identify the major product(s) in the reaction of (R)-2-bromopentane with sodium cyanide in DMSO. Please draw the correct answer choice with its stereochemistry. 6) Identify the major product(s) in the reaction of (R)-2-bromopentane with sodium cyanide in DMSO. Please draw the correct answer choice with its stereochemistry. A) B) C) D) (S)-2-cyanopentane racemic mixture of 2-cyanopentane (R)-2-cyanopentane trans-2-pentene
For number 4, I believe this is an Sn2 reaction, but unsure of the product(s). Please explain and show work, thank you! 4. (4 pts) Label the nucleophile and electrophile and draw the products of the following SN2 reaction. Be sure to indicate the appropriate stereochemistry. acetone No (CH), CO 5. (2 pts) Would the reaction above be faster or slower if each of the following substrates were used instead of trans-1-lodo-4-methylcyclohexane? a. iodoethane FASTER SLOWER FASTER b. trans-1-chloro-4-methylcyclohexane SLOWER
Draw the substitution product of the reaction of (1 S,3R)-1-chloro-3-methylcyclohexane with hydroxide.
please help Short Answer: (A) Draw all 3 steps of mechanism that gives the product 2-butene. You do not have to draw mechanisms for both products - just 2-butene (either cis or trans). Finally, clearly label each product below as the Hoffman or Zaitsev product. See Key Mechanism 7-5. ОН H2SO4 heat trans-2-butene 1-butene (C) Show ALL steps of the mechanism for the complete chlorination of 2 Cl2